Allele Registry

Canonical Allele Identifier: PA2825091866

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV003461944

ClinVar Variation:

2676808

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ser1195Gly	CA346760519 NM_000179.3:c.3583A>G